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Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic) ? Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic) ?   A)  1 > 2 > 3 B)  2 > 3 > 1 C)  3 > 2 > 1 D)  2 > 1 > 3


A) 1 > 2 > 3
B) 2 > 3 > 1
C) 3 > 2 > 1
D) 2 > 1 > 3

E) A) and D)
F) C) and D)

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What is the best choice of reagent to achieve the following reaction? What is the best choice of reagent to achieve the following reaction?   A)  Br<sub>2</sub>, CCl<sub>4</sub> B)  HBr, H<sub>2</sub>O C)  Br<sub>2</sub>, light D)  NaBr


A) Br2, CCl4
B) HBr, H2O
C) Br2, light
D) NaBr

E) A) and B)
F) A) and C)

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Which of the following compounds is aromatic?


A) ethane
B) cyclobutadiene
C) benzene
D) cyclooctatetraene

E) A) and C)
F) A) and B)

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Provide a brief explanation of why the cyclopentadienyl anion (below) is aromatic. Your answer should identify the hybridization of each carbon atom and account for which electrons are in the pi system. Provide a brief explanation of why the cyclopentadienyl anion (below) is aromatic. Your answer should identify the hybridization of each carbon atom and account for which electrons are in the pi system.

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The all five carbons are sp2 hybridized. ...

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Assuming that the sulfur atom is sp2-hybridized, there are _____ π-electrons in the sulfathiazole ring.

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Which of the following is not true about [18]annulene? Which of the following is not true about [18]annulene?   A)  [18]annulene is planar B)  [18]annulene is aromatic C)  [18]annulene gives one peak in the <sup>1</sup>H NMR spectrum D)  [18]annulene has 18 pi bonds


A) [18]annulene is planar
B) [18]annulene is aromatic
C) [18]annulene gives one peak in the 1H NMR spectrum
D) [18]annulene has 18 pi bonds

E) A) and D)
F) A) and C)

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What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?   A)  2,4-dibromotoluene B)  2,4-dibromophenol C)  2,4-dibromohydroxybenzene D)  4,6-dibromophenol


A) 2,4-dibromotoluene
B) 2,4-dibromophenol
C) 2,4-dibromohydroxybenzene
D) 4,6-dibromophenol

E) A) and D)
F) C) and D)

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What is the best choice of reagent to achieve the following reaction? What is the best choice of reagent to achieve the following reaction?   A)  H<sub>2</sub>SO<sub>4</sub> B)  NaOH, H<sub>2</sub>O C)  K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>, H<sub>2</sub>SO<sub>4</sub> D)  H<sub>2</sub>/Pd


A) H2SO4
B) NaOH, H2O
C) K2Cr2O7, H2SO4
D) H2/Pd

E) None of the above
F) B) and D)

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Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic) ? Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic) ?   A)  1 > 2 > 3 B)  2 > 1 > 3 C)  3 > 2 > 1 D)  1 > 3 > 2


A) 1 > 2 > 3
B) 2 > 1 > 3
C) 3 > 2 > 1
D) 1 > 3 > 2

E) C) and D)
F) All of the above

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How many p orbital electrons are present in cyclopentadienyl anion?


A) 4
B) 6
C) 7
D) 8

E) B) and C)
F) A) and B)

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What is the major organic product obtained from the following reaction? What is the major organic product obtained from the following reaction?   A)  1 B)  2 C)  3 D)  4


A) 1
B) 2
C) 3
D) 4

E) A) and B)
F) A) and C)

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What is the correct assignment of the names of the following heterocycles? What is the correct assignment of the names of the following heterocycles?   A)  1 = pyrrole; 2 = thiophene; 3 = pyridine B)  1 = thiophene; 2 = furan; 3 = pyrrole C)  1 = furan; 2 = pyrrole; 3 = thiophene D)  1 = furan; 2 = thiophene; 3 = pyrrole


A) 1 = pyrrole; 2 = thiophene; 3 = pyridine
B) 1 = thiophene; 2 = furan; 3 = pyrrole
C) 1 = furan; 2 = pyrrole; 3 = thiophene
D) 1 = furan; 2 = thiophene; 3 = pyrrole

E) All of the above
F) A) and C)

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What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?   A)  1-bromo-2-fluoro-4-toluene B)  4-bromo-2-fluorotoluene C)  2-bromo-4-fluorophenol D)  4-bromo-2-fluoroxylene


A) 1-bromo-2-fluoro-4-toluene
B) 4-bromo-2-fluorotoluene
C) 2-bromo-4-fluorophenol
D) 4-bromo-2-fluoroxylene

E) All of the above
F) None of the above

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What is the hybridization of the oxygen atom of furan?


A) s
B) sp
C) sp2
D) sp3

E) B) and C)
F) A) and C)

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Why are nitrophenols more acidic than phenols?

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Nitro phenols are more acidic than pheno...

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Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic) ? Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic) ?   A)  1 > 2 > 3 B)  2 > 1 > 3 C)  3 > 2 > 1 D)  1 > 3 > 2


A) 1 > 2 > 3
B) 2 > 1 > 3
C) 3 > 2 > 1
D) 1 > 3 > 2

E) None of the above
F) A) and D)

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What are the relative positions of the substituents in the following structure? What are the relative positions of the substituents in the following structure?   A)  anti B)  meta C)  ortho D)  para


A) anti
B) meta
C) ortho
D) para

E) B) and D)
F) A) and B)

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What are the relative positions of the substituents in the following structure? What are the relative positions of the substituents in the following structure?   A)  anti B)  meta C)  ortho D)  para


A) anti
B) meta
C) ortho
D) para

E) None of the above
F) B) and C)

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Consider the following structure. Consider the following structure.   -This structure contains ____ π electrons. -This structure contains ____ π electrons.

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Phenols are stronger acids than alcohols because of the resonance stabilization of alkoxide ions.

A) True
B) False

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